z-logo
Premium
Indoleninoxide, VI: Katalyse einer Isomerisierung durch Ethentetracarbonitril und Oxirantetracarbonitril
Author(s) -
Dopp Dietrich,
NourelDin Ahmed Mokhtar
Publication year - 1978
Publication title -
chemische berichte
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.667
H-Index - 136
eISSN - 1099-0682
pISSN - 0009-2940
DOI - 10.1002/cber.19781111221
Subject(s) - isomerization , chemistry , catalysis , yield (engineering) , medicinal chemistry , molar ratio , organic chemistry , materials science , metallurgy
Indolenine Oxides, VI: Catalysis of an Isomerization by Ethenetetracarbonitrile and Oxiranetetracarbonitrile Ethenetetracarbonitrile ( 2 ) or oxiranetetracarbonitrile ( 7 ), when applied in quantities of 0.1 mol per mol of 1 , are effective in isomerizing the 3H ‐indole 1‐oxide 1 into the thermodynamically more stable lactam 4 in high yield. If either 2, 7 , or tetracyanoquinodimethan ( 8 ) are applied to 1 in 1:1 molar ratios, the yields of isomerization product 4 tend to drop. — A trivial acid catalysis brought about by contamination by acidic impurities may be excluded for the isomerization of 1 by 2 .

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom